Job in Jubilant Organosys as QA / QC - Executive / Sr. Executives

Post: QA / QC - Executive / Sr. Executives

Job Description:
• Responsible for preparation and use of SOP’s in all departments as per the laid down procedures.
• Responsible for online and facility audits of QC, Production, warehouse and engineering for GMP compliance.
• Responsible for Audit of Analytical validation documents (Protocol, Report, Validation data and other supporting documents.
• Responsible for monitoring adherence to various cGMP activities and laid down procedures in receipt, storage, testing, processing and dispatch of products.
• Responsible for issuance and archival of batch manufacturing and testing records along with all second level documents till their retention period.
• Responsible for the retrieval of documents as and when required and ensure that current version of documents are available at work place.
• Preparation of approved vendor list.

Candidate Profile:
•2-5 Years experience in Pharma industry QC/Quality Assurance functions.
•Good knowledge of QA systems as per various guidelines, Hands on experience in Advance laboratory equipments & techniques like HPLC, HSGC & FTIR
•Experience and knowledge in review of Analytical Method Validation documents.
•Working experience in companies having regulatory approval from USFDA, MHRA, EDQM etc.
•Knowledge on MS Word & MS Excel
•Good Writing & Oral Communication Skills

Additional Information:
Experience: 2-5 years
Location: Mysore, Noida, Roorkee
Education: B.Sc, M.Pharm, M.Sc
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: QA/QC

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